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[Diagnostic prospects for using multilocus DNA markers in systematizing wild hooved animals (Artiodactyla)].

The possibility to use three types of molecular genetic DNA markers for studying genomic variations and differentiation in wild ungulates (exemplified by Cervidae) was estimated. DNA markers were revealed via DNA fingerprinting, taxonomic typing, and random amplification of polymorphic DNA by polymerase chain reaction (RAPD PCR). The highest polymorphism of the markers was detected in roes (Capreolus spp.) RAPD PCR appeared to be the most efficient method for diagnosis of families, genera, and species. The degree of genetic similarity between species estimated by RAPD agreed with the generally accepted taxonomy of Cervidae. DNA polymorphism and interspecies differentiation of European and Siberian roe deer (C. capreolus and C. pygargus, respectively) are discussed.

Animals↗

[Chromosomal differences in moose (Mammalia, Artiodactyla, Alces alces L.)].

Earlier studies on differences in moose (Alces alces) chromosome sets concerned only European (Scandinavia, Finland, the Volga region, and western Siberia) and American (the United States and Canada) forms. The first group had a 68-chromosome set, and the second group, a 70-chromosome set. These differences were considered interspecies chromosomal polymorphism. However, the chromosome number in A. alces living in eastern and northeastern Siberia remains unknown, although these data are important for elucidation of the geographical variation of karyotypes of moose from genus Alces. Four moose from different regions of Sakha were studied. It was found that their karyotypes contained 70 chromosomes; i.e., they were similar to the American form. These data indicate a strong differentiation within the species. Two chromosomal forms can be distinguished: the European one (2n = 68) living in Europe and western Siberia and the American one (2n = 70) living in North America, the Far East, and eastern Siberia. The existence of two forms is confirmed by data on their morphology, sound signals, electrophoretic mobility of proteins, and differences in nutrition. These results indicate that long-term isolation of European and American moose led to the high divergence between these two forms; therefore, they can be considered different species.

Animals↗

The tribal radiation of the family Bovidae (Artiodactyla) and the evolution of the mitochondrial cytochrome b gene.

The nucleotide sequence of the complete mitochondrial cytochrome b gene has been determined and compared for 51 species of the family Bovidae and 10 potential pecoran and tragulid outgroups. A detailed saturation analysis at each codon position relative to the maximum parsimony procedure indicates that all transitions on third codon positions do not accumulate in a similar fashion: C-T are more saturated than A-G substitutions. The same trend is observed for second positions but not for first positions where A-G and C-T transitions exhibit roughly the same levels of saturation. Maximum parsimony reconstructions were weighted according to these observations. Maximum parsimony, maximum likelihood, and distance phylogenetic reconstructions all depict a major split within Bovidae. The subfamily Bovinae includes four multifurcating tribes and subtribes: Boselaphini, Tragelaphini, cattle-Bovini (Bos and Bison), and buffalo-Bovini (Bubalus and Syncerus). Its sister group is the subfamily Antilopinae, i.e., all non-Bovinae taxa, represented by seven lineages: Antilopini (including Saiga), Caprini sensu lato (i. e., Caprinae including Pantholops), Hippotragini, Alcelaphini, Reduncini (including Pelea), Aepyceros possibly linked to Neotragus, and Cephalophini possibly linked to Oreotragus (the suni and the klipspringer being members of a polyphyletic Neotragini). These various tribes and major lineages were produced by two noteworthy explosive radiations, which occurred simultaneously between 12.0 and 15.3 MY (Middle Miocene) in the subfamilies Bovinae and Antilopinae.

Animals↗

Meiosis in chromosomally heteromorphic goitered gazelle, Gazella subgutturosa (Artiodactyla, Bovidae).

Chromosomal-pairing behaviour was studied in the spermatocytes of individual goitered gazelles which were heteromorphic for a 14/15 Robertsonian translocation and which possessed an autosome-to-X translocation. Both translocations exhibited trivalent pairing configurations in pachytene and diakinesis/metaphase I nuclei. Synapsis of the sex chromosomes during pachynema was followed by end-to-end association of the X and Y during diakinesis/metaphase I. The only univalents identified were of the Y chromosome; Y univalency ranged from 15.9% at pachynema to 5.7% at diakinesis/metaphase I. Robertsonian trivalents exhibited evidence of synaptic adjustment in the paracentromeric region. Chiasmata were formed in most bivalents and trivalents; chiasmata were restricted to the autosomal portion of the autosome-to-XY trivalent. Analysis of metaphase II configurations (secondary spermatocytes) revealed no nondisjunction in individuals homozygous or heterozygous for the Robertsonian translocation. These data are consistent with the hypothesis that neither the autosomal nor the gonosomal heteromorphism reduces the meiotic fitness of male goitered gazelles.

Animals↗

Chromosomes of Damaliscus (Artiodactyla, Bovidae): simple and complex centric fusion rearrangements.

G- and C-banded karyotypes of Damaliscus hunteri, D. lunatus and D. pygargus were compared using the standard karyotype of Bos taurus. Chromosomal complements were 2n = 36 in D. lunatus jimela, 2n = 38 in D. pygargus phillipsi and D. p. pygargus, and 2n = 44 in D. hunteri. The fundamental number in all karyotypes was 60. Among the three species of Damaliscus, seven autosomal pairs and the X chromosomes were conserved. Y-chromosome differences were attributed to heterochromatic additions or deletions. Banded karyotypes of the two subspecies of D. pygargus exhibited complete homology. Chromosomal complements of D. pygargus and D. lunatus differed by a simple centric fusion. However, karyotypes of D. pygargus and D. lunatus differed from D. hunteri by numerous centric fusions, several of which were related by monobrachial chain complexes. Between the karyotypes of D. hunteri and D. pygargus or D. lunatus, there were two chain complexes, one involving five chromosomes (chain V) and the other involving 12 in pygargus (chain XII) or 13 in lunatus (chain XIII). There were also two simple centric fusions between D. hunteri and D. lunatus/D. pygargus; acrocentric chromosomes 13, 15, 20 and 22 in D hunteri were fused as 13;15 and 20;22 in D. lunatus and D. pygargus.

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Evolutionary history of the genus Capra (Mammalia, Artiodactyla): discordance between mitochondrial DNA and Y-chromosome phylogenies.

The systematics of the genus Capra remain controversial in spite of studies conducted using morphology, mtDNA, and allozymes. Here, we assess the evolutionary history of Capra (i) using phylogenetic analysis of two nuclear genes located on the Y-chromosome and (ii) previously published and new cytochrome b sequences. For the Y-chromosome phylogeny, we sequenced segments from the amelogenin (AMELY) and zinc finger (ZFY) genes from all of the eight wild taxa and from domestic goats (Capra hircus). Phylogenetic analysis of the Y-chromosome data revealed two well-defined clades. The domestic goat (C. hircus), the bezoar (Capra aegagrus), and the markhor (C. falconeri) belong to one clade (ML bootstrap value [BP]: 98%), suggesting that domestic goats originated from one or both of these wild species. The second clade (ML BP: 92%) is comprised of all the other wild species. Horn morphology is generally concordant with the Y-chromosome phylogeny. The mtDNA data also revealed two well-defined clades. However, the species in each clade are different from those inferred from the Y-chromosome data. To explain the discordance between Y-chromosome and mtDNA phylogenies, several hypotheses are considered. We suggest that a plausible scenario involves mtDNA introgression between ancestral taxa before the relatively recent colonization of Western Europe, the Caucasus Mountains, and East Africa by Capra populations.

Africa↗

The macroscopic and microscopic structure of double-head antlers and pedicle bone of cervidae (Mammalia, Artiodactyla).

Ortho- and heterotopically formed double-head antlers were studied in red, fallow and roe deer. The malformation was the result of new antler growth without previous casting of the old antlers. Thus, two antler structures belonging to successive antler generations originated from one pedicle. These two structures were always separated by a horizontal groove. Histologically, signs of osteoclastic resorption were observed in the interior and at the outer circumference of the distal parts of the pedicles of the double heads. The resorptive process had, however, not been of an intensity necessary for subsequent antler casting. We also observed that the double-head's second antler generation had developed as a periosteal exostosis of the distal pedicle bone. Thus, we assume that in normogenesis formation of the bony component of subsequent antlers is also probably dependent on cells derived from pedicle periosteum. Finally, the process of antler regrowth in deer is compared with epimorphic regeneration occurring in other vertebrates.

Animals↗

A karyotypic analysis of nilgai, Boselaphus tragocamelus (Artiodactyla: Bovidae).

A combination of chromosomal banding and fluorescence in situ hybridization (FISH) was used to characterize the karyotype of Boselaphus tragocamelus (nilgai) relative to the domestic cattle standard karyotype. G-, Q- and C-band karyotypes of nilgai are presented, and the chromosomal complement of nilgai is determined to be 2n=46 (female FN=60, male FN=59; NAA=56), consistent with previous reports for the species. Comparisons with cattle identified extensive monobrachial homologies with some noteworthy exceptions. Chromosome 25 is centrically fused to 24, and chromosome 16 is acrocentric. Both appear to have additional pericentromeric material not seen in the equivalent cattle acrocentrics. This pericentromeric chromatin may be the result of de novo additions or translocation of pericentromeric material from chromosome 6, which is shown to be centrically fused to 13 but is only about two-thirds the length of cattle 6. Comparisons with cattle demonstrated that nilgai chromosome 17 has undergone a paracentric inversion and that chromosome 20 has two blocks of interstitial constitutive heterochromatin. The identities of both chromosomes were confirmed by chromosomal FISH. Furthermore, chromosomal banding and FISH were used to determine that autosome 14 has been fused to the ancestral X and Y of nilgai to form compound neo-X and -Y chromosomes. Additional FISH analyses were conducted to confirm other proposed chromosome homologies and to identify nucleolar organizing regions within the nilgai complement.

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